Quality Assurance Pharma

Amaris Consulting; Frosinone; In loco; EUR 35.000 - 45.000; Tempo pieno

Descrizione del lavoro

A fast-growing consulting company in Frosinone is seeking a dedicated Quality Assurance Associate. In this role, you will support the Supplier Quality organization by managing supplier activities and ensuring compliance with quality standards. Candidates should have a scientific degree and proficiency in English. The position offers an international and multicultural environment with growth opportunities and training programs, contributing to innovative projects in the Life Sciences sector.

Servizi

International and multicultural work environment

Clear career path with personalized growth opportunities

Continuous training and development programs

Opportunity to contribute to innovative projects

Competenze

• Experience managing and overseeing GMP deviations, including investigation and documentation.
• Coordinate and review root cause analysis and risk assessments.
• Define, track, and close CAPAs ensuring effectiveness and timely implementation.

Mansioni

• Maintain and update records related to external suppliers, including materials and qualifications.
• Assist in supplier assessments and manage supplier documentation.
• Manage and oversee GMP deviations, including investigation and documentation.
• Collaborate on projects as part of a team.

Conoscenze

Proficiency in English

Strong organizational skills

Excellent written and verbal communication skills

Attention to detail

Ability to work collaboratively

Formazione

Scientific degree in Pharmaceutical Sciences, Biology, Chemistry or related area

Descrizione del lavoro

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Job Description

We are seeking a dedicated and detail-oriented Quality Assurance Associate to join our team in Frosinone. The successful candidate will play a crucial role in supporting the Supplier Quality organization by managing supplier‑related activities and ensuring compliance with quality standards.

Responsibilities

• Maintain and update records related to external suppliers, including information on materials, qualifications, and monitoring activities.
• Assist in supplier assessments and manage supplier documentation, including specifications agreements.
• Manage and oversee GMP deviations, including investigation and documentation.
• Follow‑up on activities related to supplier performance.
• Support change control processes to ensure effective management of supplier changes.
• Assist in the management and follow‑up of activities related to EQ‑SQ/Supplier investigations and Corrective and Preventive Actions (CAPA).
• Collaborate on projects as part of a team.

Qualifications

• Scientific degree in a relevant field (Pharmaceutical Sciences, Biology, Chemistry, or related area).
• Proficiency in English (mandatory).
• Experience managing and overseeing GMP deviations, including investigation and documentation.
• Coordinate and review root cause analysis and risk assessments.
• Define, track, and close CAPAs, ensuring effectiveness and timely implementation.
• Monitor deviation and CAPA trends to identify systemic issues.
• Ensure compliance with GMP requirements and support audits and inspections.
• Strong organizational skills and attention to detail.
• Ability to work collaboratively in a team environment.
• Excellent written and verbal communication skills.

Benefits

• An international and multicultural work environment within a fast‑growing consulting company.
• A clear career path with personalized growth opportunities (both vertical and horizontal).
• Continuous training and development programs through our internal Academy.
• The opportunity to contribute to innovative projects with leading international clients in the Life Sciences sector.

At Amaris Consulting, we believe that diversity is a strength and we are proud to be an equal opportunities employer. We welcome applications from all backgrounds and are committed to fostering an inclusive environment where every voice is heard and valued.